Literature DB >> 11810186

Reversible coma with raised intracranial pressure: an unusual clinical manifestation of CADASIL.

F Feuerhake1, B Volk, C B Ostertag, F D Jungling, J Kassubek, M Orszagh, M Dichgans.   

Abstract

A 50-year-old woman presented with recurrent episodes of headache, nausea and disturbed consciousness that were fully reversible within a few days. Clinical and radiological findings suggested raised intracranial pressure, which on one occasion was confirmed by intracranial pressure monitoring. Magnetic resonance imaging performed in the asymptomatic interval disclosed a diffuse leukoencephalopathy. Brain biopsy surprisingly revealed the typical vascular changes of CADASIL and subtle endothelial alterations. The white matter showed edematous changes and reactive gliosis. Mutational analysis of the Notch3 gene revealed a previously unreported mutation. We suggest that a transient disturbance of the blood-brain barrier related to the underlying vascular pathology may have caused this unusual presentation of CADASIL.

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Year:  2001        PMID: 11810186     DOI: 10.1007/s004010100439

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  11 in total

Review 1.  CADASIL: Imaging Characteristics and Clinical Correlation.

Authors:  Shuhan Zhu; Stephanie J Nahas
Journal:  Curr Pain Headache Rep       Date:  2016-10

2.  Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy syndrome mutations increase susceptibility to spreading depression.

Authors:  Katharina Eikermann-Haerter; Izumi Yuzawa; Ergin Dilekoz; Anne Joutel; Michael A Moskowitz; Cenk Ayata
Journal:  Ann Neurol       Date:  2011-02       Impact factor: 10.422

3.  "CADASIL coma" in an Italian homozygous CADASIL patient: comparison with clinical and MRI findings in age-matched heterozygous patients with the same G528C NOTCH3 mutation.

Authors:  Michele Ragno; Luigi Pianese; Manrico Morroni; Gabriella Cacchiò; Antonio Manca; Fabio Di Marzio; Serena Silvestri; Cristina Miceli; Maria Scarcella; Marco Onofrj; Luigi Trojano
Journal:  Neurol Sci       Date:  2013-04-10       Impact factor: 3.307

Review 4.  Migraine headache: a review of the molecular genetics of a common disorder.

Authors:  Cherubino Di Lorenzo; Gaetano S Grieco; Filippo M Santorelli
Journal:  J Headache Pain       Date:  2012-09-01       Impact factor: 7.277

Review 5.  Neuropsychiatric manifestations in CADASIL.

Authors:  Hugues Chabriat; Marie-Germaine Bousser
Journal:  Dialogues Clin Neurosci       Date:  2007       Impact factor: 5.986

6.  Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in an Israeli family.

Authors:  Radi Shahien; Silvia Bianchi; Abdalla Bowirrat
Journal:  Neuropsychiatr Dis Treat       Date:  2011-06-20       Impact factor: 2.570

Review 7.  Genetics of cerebral small vessel disease.

Authors:  Jay Chol Choi
Journal:  J Stroke       Date:  2015-01-30       Impact factor: 6.967

8.  Cadasil coma: Unusual cause for acute encephalopathy.

Authors:  Venkatesan Prasanna Eswaradass; Balakrishnan Ramasamy; Ramadoss Kalidoss; Gnanashanmugham Gnanagurusamy
Journal:  Ann Indian Acad Neurol       Date:  2015 Oct-Dec       Impact factor: 1.383

9.  The First Report of CADASIL in Peru: Olfactory Dysfunction on Initial Presentation.

Authors:  Anastasia Vishnevetsky; Miguel Inca-Martinez; Karina Milla-Neyra; Danny Moises Barrientos-Iman; Ivan Cornejo-Herrera; Carlos Cosentino; Mario Cornejo-Olivas
Journal:  eNeurologicalSci       Date:  2016-09-28

Review 10.  Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy revisited: Genotype-phenotype correlations of all published cases.

Authors:  Georgia Xiromerisiou; Chrysoula Marogianni; Katerina Dadouli; Christina Zompola; Despoina Georgouli; Antonios Provatas; Aikaterini Theodorou; Paschalis Zervas; Christina Nikolaidou; Stergios Stergiou; Panagiotis Ntellas; Maria Sokratous; Pantelis Stathis; Georgios P Paraskevas; Anastasios Bonakis; Konstantinos Voumvourakis; Christos Hadjichristodoulou; Georgios M Hadjigeorgiou; Georgios Tsivgoulis
Journal:  Neurol Genet       Date:  2020-05-11
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